材料科学
晶界
钙钛矿(结构)
铆钉
偶极子
能量转换效率
光伏系统
电荷(物理)
光电子学
限制
双功能
粒度
平面的
卤化物
复合材料
钙钛矿太阳能电池
电压
晶粒生长
工程物理
俘获
纳米技术
动能
化学工程
作者
Yifan Niu,Zuhong Zhang,Congcong Zhang,Jorge Pascual,Weiwei Zuo,Ying Tang,Hongzhuo Wu,Zhenhuang Su,Mahmoud H. Aldamasy,Rui Zhu,Meng Li
摘要
ABSTRACT The formation of grain boundaries and grooves inherent to perovskite films severely hinders interfacial charge extraction and induces non‐radiative recombination, thereby limiting both photovoltaic efficiency and long‐term stability of devices. Here, we introduce a dual‐site locking strategy using a bifunctional molecule, 4‐chloro‐phenethylammonium halide (4Cl‐PEAX, X═Cl, Br, I), to simultaneously anchor Pb and I sites at the grain boundaries. This locking effectively rivets the grain boundary grooves (GBGs), creating a compact, flattened, and energetically well‐aligned interface that promotes charge transport and suppresses non‐radiative losses. Among the series, 4Cl‐PEAI, with the highest dipole moment, delivers the greatest improvement, yielding p‐i‐n perovskite solar cells (PSCs) with a power conversion efficiency (PCE) of 26.73% with an open‐circuit voltage ( V OC ) of 1.20 V and a fill factor (FF) of 86%, while retaining over 90% of their initial efficiency after prolonged storage and continuous operation. This dual‐site interfacial riveting approach offers a general design principle for enhancing the mechanical and chemical stability of high‐performance perovskite photovoltaics.
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